Chemistry and Biochemistry Department, University of Maryland, Baltimore County, Baltimore, Maryland, United States of America.
Institute of Fluorescence, University of Maryland, Baltimore County, Baltimore, Maryland, United States of America.
PLoS One. 2019 Sep 30;14(9):e0223008. doi: 10.1371/journal.pone.0223008. eCollection 2019.
Nucleases are enzymes that can degrade genomic DNA and RNA that decrease the accuracy of quantitative measures of those nucleic acids. Here, we study conventional heating, standard microwave irradiation, and Lyse-It, a microwave-based lysing technology, for the potential to fragment and inactivate DNA and RNA endonucleases. Lyse-It employs the use of highly focused microwave irradiation to the sample ultimately fragmenting and inactivating RNase A, RNase B, and DNase I. Nuclease size and fragmentation were determined visually and quantitatively by SDS polyacrylamide gel electrophoresis and the mini-gel Agilent 2100 Bioanalyzer system, with a weighted size calculated to depict the wide range of nuclease fragmentation. Enzyme activity assays were conducted, and the rates were calculated to determine the effect of various lysing conditions on each of the nucleases. The results shown in this paper clearly demonstrate that Lyse-It is a rapid and highly efficient way to degrade and inactivate nucleases so that nucleic acids can be retained for down-stream detection.
核酸酶是能够降解基因组 DNA 和 RNA 的酶,这会降低这些核酸定量测量的准确性。在这里,我们研究了常规加热、标准微波辐射以及基于微波的裂解技术 Lyse-It,以评估它们潜在的断裂和失活 DNA 和 RNA 内切酶的能力。Lyse-It 采用高度聚焦的微波辐射来对样品进行处理,最终会使 RNase A、RNase B 和 DNase I 断裂失活。通过 SDS 聚丙烯酰胺凝胶电泳和安捷伦 2100 生物分析仪系统进行视觉和定量的核酸酶大小和片段化检测,计算出加权大小以描绘核酸酶片段化的广泛范围。进行了酶活性测定,并计算了速率,以确定各种裂解条件对每种核酸酶的影响。本文中的结果清楚地表明,Lyse-It 是一种快速且高效的降解和失活核酸酶的方法,以便可以保留核酸进行下游检测。